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Thursday, February 22, 2018

Figure 4 | Journal of Medical Genetics
src: jmg.bmj.com

Albright's hereditary osteodystrophy is a form of osteodystrophy, and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone.


Video Albright's hereditary osteodystrophy



Signs/symptoms

The disorder is characterized by the following:

  • Hypogonadism
  • Brachydactyly syndrome
  • Choroid plexus calcification
  • Hypoplasia of dental enamel
  • Full cheeks
  • Hypocalcemic tetany

Individuals with Albright hereditary osteodystrophy exhibit short stature, characteristically shortened fourth and fifth metacarpals, rounded facies, and often mild intellectual deficiency. Albright hereditary osteodystrophy is commonly known as pseudohypoparathyroidism because the kidney responds as if parathyroid hormone were absent. Blood levels of parathyroid hormone are elevated in pseudohypoparathyroidism due to the hypocalcemia


Maps Albright's hereditary osteodystrophy



Genetics

This condition is associated with genetic imprinting. It is thought to be inherited in an autosomal dominant pattern, and seems to be associated with a Gs alpha subunit deficiency.


Mendelism, Patterns of Human Inheritance By: Mahdi Bijanzadeh MD ...
src: slideplayer.com


Mechanism

The mechanism of this condition is due to Gs signaling decrease in hormones having to do with signal transduction which is when a signal from outside cell causes change within the cell (in function). Renal tubular cells don't expresses paternal only maternal alleles(variant form of a gene).


SHORT STATURE MZ.Zamanpour MD. Normal Growth  Normal growth: A ...
src: images.slideplayer.com


Diagnosis

The diagnosis of Albright's hereditary osteodystrophy is based on the following exams below:

  • CBC
  • Urine test
  • MRI

Pseudohypoparathyroidism - Basic Science - Orthobullets
src: upload.orthobullets.com


Treatment

Treatment consists of maintaining normal levels of calcium, phosphorus, and vitamin D. Phosphate binders, supplementary calcium and vitamin D will be used as required.


Parathyroid Disorders | Article, Article, Articles | Pediatrics in ...
src: pedsinreview.aappublications.org


History

The disorder bears the name of Fuller Albright, who characterized it in 1942. He was also responsible for naming it "Sebright bantam syndrome," after the Sebright bantam chicken, which demonstrates an analogous hormone insensitivity. Much less commonly, the term Martin-Albright syndrome is used, this refers to Eric Martin.


Genetics of congenital hypothyroidism | Journal of Medical Genetics
src: jmg.bmj.com


See also

  • Pseudopseudohypoparathyroidism

Brachydactyly | Orphanet Journal of Rare Diseases | Full Text
src: media.springernature.com


References


Achondroplasia - Wikipedia
src: upload.wikimedia.org


Further reading

  • Thakker, Rajesh V.; Whyte, Michael P.; Eisman, John; Igarashi, Takashi (2013). Genetics of Bone Biology and Skeletal Disease. Academic Press. ISBN 9780123878304. Retrieved 12 February 2017. 
  • Henderson, Katherine E.; Baranski, Thomas J.; Bickel, Perry E.; Clutter, William E. (2009). The Washington Manual Endocrinology Subspecialty Consult. Lippincott Williams & Wilkins. ISBN 9780781791540. Retrieved 12 February 2017. 

J Endocrinol Metab
src: www.jofem.org


External links



Source of article : Wikipedia